HRID1191927

反应详情

EQUATION

反应方程式

HRID 1191927 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
95 °C

PROCEDURE

实验过程

A mixture of 4-(trifluoromethyl)-6,6a-dihydro-1aH-indeno[1,2-b]oxirene (1.2 g, 6.0 mmol) and tert-butyl (3S)-3-methylpiperazine-1-carboxylate (1.4 g, 7.2 mol) in ethanol (20 mL) was refluxed overnight. Another gram of tert-butyl (3S)-3-methylpiperazine-1-carboxylate was added. The mixture was transferred into a sealed flask and heated to 95° C. for 2 days. The solvent was concentrated and the residue was purified by flash chromatography eluting with 25% EtOAc/hexane, followed by 5% MeOH/EtOAc+0.5% concentrated NH4OH. Two isomers were isolated. Isomer 1 (fast moving isomer): 0.45 g; MS calculated for the C20H27F3N2O3 (M+H)+ 401. found 401.1. Isomer 2 (slow moving isomer): 0.38 g; MS found 401.1.

WORKUP

后处理

  1. temperaturewas refluxed overnight
  2. customThe mixture was transferred into a sealed flask
  3. concentrationThe solvent was concentrated
  4. customthe residue was purified by flash chromatography
  5. washeluting with 25% EtOAc/hexane
  6. customTwo isomers were isolated